Evaluation of trends and prognosis over time in patients with AML relapsing after allogeneic hematopoietic cell transplant reveals improved survival for young patients in recent years
| dc.contributor.author | Bazarbachi, Ali Abdul Hamid | |
| dc.contributor.author | Schmid, Christof C. | |
| dc.contributor.author | Labopin, Myriam | |
| dc.contributor.author | Beelen, Dietrich Wilhelm | |
| dc.contributor.author | Blau, Igor Wolfgang | |
| dc.contributor.author | Potter, Victoria T. | |
| dc.contributor.author | Niittyvuopio, Riitta | |
| dc.contributor.author | Socié, Gérard A. | |
| dc.contributor.author | Blaise, Didier P. | |
| dc.contributor.author | Sanz, Jaime | |
| dc.contributor.author | Ciceri, Fabio | |
| dc.contributor.author | Abou Dalle, Iman | |
| dc.contributor.author | Spyridonidis, Alexandros | |
| dc.contributor.author | Bug, Gesine | |
| dc.contributor.author | Estève, Jordi | |
| dc.contributor.author | Savani, Bipin N. | |
| dc.contributor.author | Nagler, Arnon | |
| dc.contributor.author | Mohty, Mohamad | |
| dc.contributor.department | Specialized Clinical Programs and Services | |
| dc.contributor.department | Internal Medicine | |
| dc.contributor.department | Bone Marrow Transplantation (BMT) Program | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T12:20:32Z | |
| dc.date.available | 2025-01-24T12:20:32Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | Purpose: Relapsed acute myeloid leukemia (AML) post allogeneic hematopoietic cell transplantation (allo-HCT) has a dismal prognosis. Experimental Design: To assess prognosis of patients with recurrent AML post allo-HCT over time, we analyzed European Society for Blood and Marrow Transplantation registry data of 8,162 adult patients with AML who relapsed between 2000 and 2018 after allo-HCT performed in first complete remission from matched sibling, unrelated, or haploidentical donors. Results: The 2-year overall survival (OS) rate from relapse was 17%. For 3,630 patients, <50 years of age, the 2-year OS continuously increased from 16% between 2000 and 2004 to 18% for 2005-2009, to 21% for 2010-2014, and to 26% for 2015-2018 (P ¼ 0.001). Improvement over time was noted both after relapse within and beyond 6 months from allo-HCT. On multivariate analysis among patients <50 years of age, OS was positively affected by a later year of relapse (baseline: 2000-2004; HR, 0.82; P < 0.02 for 2010-2014 and HR, 0.72; P ¼ 0.0002 for 2015-2018), good performance status, favorable cytogenetics, and longer time from transplant to relapse, but negatively affected by increasing age. In contrast, among 4,532 patients, >50 years of age, the year of relapse had no influence on OS (16% for 2000-2004 and 14% for 2015-2018; P ¼ 0.56). Regarding treatment, encouraging results were observed after second allo-HCT, which was performed within 2 years after relapse in 17% of the entire cohort, resulting in a 2-year OS of 30.7%. Conclusions: Outcome after posttransplant relapse among younger patients has improved significantly in recent years, likely reflecting, among other factors, the efficacy of posttransplant salvage including second allo-HCT. © 2020 American Association for Cancer Research. | |
| dc.identifier.doi | https://doi.org/10.1158/1078-0432.CCR-20-3134 | |
| dc.identifier.eid | 2-s2.0-85100887091 | |
| dc.identifier.pmid | 32988970 | |
| dc.identifier.uri | http://hdl.handle.net/10938/34322 | |
| dc.language.iso | en | |
| dc.publisher | American Association for Cancer Research Inc. | |
| dc.relation.ispartof | Clinical Cancer Research | |
| dc.source | Scopus | |
| dc.subject | Adolescent | |
| dc.subject | Adult | |
| dc.subject | Age factors | |
| dc.subject | Aged | |
| dc.subject | Aged, 80 and over | |
| dc.subject | Female | |
| dc.subject | Follow-up studies | |
| dc.subject | Hematopoietic stem cell transplantation | |
| dc.subject | Humans | |
| dc.subject | Leukemia, myeloid, acute | |
| dc.subject | Male | |
| dc.subject | Middle aged | |
| dc.subject | Mortality | |
| dc.subject | Neoplasm recurrence, local | |
| dc.subject | Prognosis | |
| dc.subject | Remission induction | |
| dc.subject | Retrospective studies | |
| dc.subject | Salvage therapy | |
| dc.subject | Survival rate | |
| dc.subject | Transplantation, homologous | |
| dc.subject | Young adult | |
| dc.subject | Busulfan | |
| dc.subject | Cd135 antigen | |
| dc.subject | Cyclophosphamide | |
| dc.subject | Granulocyte colony stimulating factor | |
| dc.subject | Nucleophosmin | |
| dc.subject | Acute graft versus host disease | |
| dc.subject | Acute myeloid leukemia | |
| dc.subject | Age | |
| dc.subject | Allogeneic hematopoietic stem cell transplantation | |
| dc.subject | Article | |
| dc.subject | Cancer patient | |
| dc.subject | Cancer prognosis | |
| dc.subject | Cancer registry | |
| dc.subject | Cancer survival | |
| dc.subject | Cause of death | |
| dc.subject | Chronic graft versus host disease | |
| dc.subject | Cohort analysis | |
| dc.subject | Controlled study | |
| dc.subject | Cytogenetics | |
| dc.subject | Cytomegalovirus infection | |
| dc.subject | Europe | |
| dc.subject | Flt3 gene | |
| dc.subject | Follow up | |
| dc.subject | Haploidentical donor | |
| dc.subject | Human | |
| dc.subject | Human cell | |
| dc.subject | Leukemia relapse | |
| dc.subject | Leukemia remission | |
| dc.subject | Major clinical study | |
| dc.subject | Multivariate analysis | |
| dc.subject | Npm1 gene | |
| dc.subject | Overall survival | |
| dc.subject | Retrospective study | |
| dc.subject | Sibling donor | |
| dc.subject | Trend study | |
| dc.subject | Unrelated donor | |
| dc.subject | Allotransplantation | |
| dc.subject | Clinical trial | |
| dc.subject | Multicenter study | |
| dc.subject | Pathology | |
| dc.subject | Remission | |
| dc.subject | Tumor recurrence | |
| dc.subject | Very elderly | |
| dc.title | Evaluation of trends and prognosis over time in patients with AML relapsing after allogeneic hematopoietic cell transplant reveals improved survival for young patients in recent years | |
| dc.type | Article |
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